Canonical Allele Identifier: CA2259640372
Gene: SMARCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40628460T= , CM000679.2:g.40628460T= GRCh38
NC_000017.10:g.38784712T= , CM000679.1:g.38784712T= GRCh37
NC_000017.9:g.36038238T= NCBI36
NG_032163.1:g.24392A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264640.9:c.*1123A= ENSP00000466608.2:n.*1123A=
ENST00000348513.12:c.*325A= MANE Select ENSP00000323967.6:n.*325A=
ENST00000377808.9:c.*548A= ENSP00000367039.4:n.*548A=
ENST00000400122.8:c.*548A= ENSP00000411607.2:n.*548A=
ENST00000469334.6:n.2159A=
ENST00000578112.6:c.*1358A= ENSP00000464501.1:n.*1358A=
ENST00000580419.6:c.*540A= ENSP00000462475.2:n.*540A=
ENST00000642576.1:n.2704A=
ENST00000643030.1:n.2184A=
ENST00000643255.1:c.*3625A= ENSP00000493957.1:n.*3625A=
ENST00000643318.1:c.*325A= ENSP00000494771.1:n.*325A=
ENST00000643378.1:n.2116A=
ENST00000643683.1:c.*325A= ENSP00000496094.1:n.*325A=
ENST00000643893.1:n.1854A=
ENST00000644443.1:n.3449A=
ENST00000644523.1:n.1607A=
ENST00000644527.1:c.*325A= ENSP00000493974.1:n.*325A=
ENST00000644701.1:c.*548A= ENSP00000496097.1:n.*548A=
ENST00000644909.1:c.*830A= ENSP00000493649.1:n.*830A=
ENST00000645152.1:n.2224A=
ENST00000645227.1:c.*1249A= ENSP00000495021.1:n.*1249A=
ENST00000646242.1:n.7473A=
ENST00000646283.1:c.*325A= ENSP00000494537.1:n.*325A=
ENST00000646401.1:n.2927A=
ENST00000646856.1:c.*1437A= ENSP00000494505.1:n.*1437A=
ENST00000647294.1:c.*1491A= ENSP00000494815.1:n.*1491A=
ENST00000647508.1:c.*325A= ENSP00000496445.1:n.*325A=
ENST00000647515.1:c.*1092A= ENSP00000495857.1:n.*1092A=
ENST00000348513.10:c.*325A= ENSP00000323967.6:n.*325A=
ENST00000578112.5:c.*1358A= ENSP00000464501.1:n.*1358A=
NM_003079.4:c.*325A= NP_003070.3:n.*325A=
NM_003079.5:c.*325A= MANE Select NP_003070.3:n.*325A=